TransEar

Primary DI
08103230003802
Brand
TransEar
Company
EAR TECHNOLOGY CORPORATION
Model
TE380
Catalog number
none
Device description
bone conduction hearing aid -
Published
2016-10-06
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
LXBHearing Aid, Bone Conduction

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXBHearing Aid, Bone ConductionEar, Nose, Throat2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K050653000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K050653000TRANSEAR BONE CONDUCTION HEARING AIDUnited Hearing Systems, Inc.2005-07-01LXB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08103230003802PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08103230003802081032300038028103230003802

GMDN Terms#

Term, Definition table
TermDefinition
Bone vibratorAn electromechanical transducer intended to produce the sensation of hearing by vibrating the cranial bones. It can be used as an output device with an audiometer to measure bone-conduction hearing thresholds, and thus serve as an adjunct to air-conduction testing with conventional earphones. Comparison of the results enables the clinician to distinguish hearing loss attributable to the external or middle ear (conductive loss) from the inner ear (sensory loss). In addition, this device may be used to provide output for a hearing aid for patients who cannot wear an earmould.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
023930584
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810323000003LightBeamLB10-refill2024-01-31
00810323009631TweakFocus+T otc2023-08-14
00810323001918LightBeamLB05-Refill2023-06-01
00810323001840LightBeamLB04-Refill2022-05-09
00810323001857LightBeamLB05-Refill2022-05-09
00810323001864LightBeamLB06-Refill2022-05-09
00810323001871LightBeamLB07-Refill2022-05-09
00810323001888LightBeamLB08-Refill2022-05-09
00810323001895LightBeamLB09-Refill2022-05-09
00810323001901LightBeamLB-Variety2022-05-09
00810323005718LightBeamLB-Charger2022-05-09
00810323005725LightBeamLB-LSO2022-05-09
00810323005732LightBeamLB-Magnifier2022-05-09
00810323001802LightBeamLB-Complete2022-05-06
00810323001819LightBeamLB01-Refill2022-05-06
00810323001826LightBeamLB02-Refill2022-05-06
00810323001833LightBeamLB03-Refill2022-05-06
00810323002540ClikClik2020-02-11
00810323003806TransEarTE380none2016-10-06
08103230025453ClikClik2020-02-11

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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